1-Butene, 2-methyl-4-[(3-methyl-2-butenyl)oxy]-

Base Information

• Chemical Name: 1-Butene, 2-methyl-4-[(3-methyl-2-butenyl)oxy]-
• CAS No.: 59637-41-1
• Molecular Formula: C10H18 O
• Molecular Weight: 154.252
• European Community (EC) Number: 261-829-3
• UNII: T9N6YC888T
• DSSTox Substance ID: DTXSID9069342
• Nikkaji Number: J298.194G
• Mol file: 59637-41-1.mol

Synonyms:59637-41-1;Bis-gamma, gamma-dimethylallyl ether;1-Butene, 2-methyl-4-[(3-methyl-2-butenyl)oxy]-;2-methyl-4-[(3-methyl-2-butenyl)oxy]but-1-ene;2-Methyl-4-((3-methyl-2-butenyl)oxy)but-1-ene;T9N6YC888T;EINECS 261-829-3;1-Butene, 2-methyl-4-((3-methyl-2-butenyl)oxy)-;2-Butene, 3-methyl-1-((3-methyl-3-buten-1-yl)oxy)-;3-methyl-1-(3-methylbut-3-enoxy)but-2-ene;UNII-T9N6YC888T;DTXSID9069342;SCHEMBL11135438;Bis-.gamma., .gamma.-dimethylallyl ether;3-Methyl-3-butenyl 3-methyl-2-butenyl ether;2-Methyl-4-[(3-methyl-2-butenyl)oxy]-1-butene;2-Methyl-4-[(3-methyl-2-butenyl)oxy]-1-butene #;3-Methyl-1-[(3-methyl-3-buten-1-yl)oxy]-2-butene

Chemical Property of 1-Butene, 2-methyl-4-[(3-methyl-2-butenyl)oxy]-

Chemical Property:

• Vapor Pressure: 0.689mmHg at 25°C
• Boiling Point: 192.2°C at 760 mmHg
• Flash Point: 56.3°C
• PSA: 9.23000
• Density: 0.819g/cm³
• LogP: 2.93540
• XLogP3: 3.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 154.135765193
• Heavy Atom Count: 11
• Complexity: 141

Purity/Quality:

98%Min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=CCOCCC(=C)C)C

Technology Process of 1-Butene, 2-methyl-4-[(3-methyl-2-butenyl)oxy]-

There total 2 articles about 1-Butene, 2-methyl-4-[(3-methyl-2-butenyl)oxy]- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 5.0%

3-methyl-2-buten-1-ol (556-82-1) → (+/-)-lavandulol (58461-27-1,21090-68-6) + 1-(3,3-dimethyl-2-propen-1-yl) oxy-3-methyl-3-butene (59637-41-1)

Guidance literature:

With Montmorillonite K 10; Ambient temperature;

DOI:10.1016/S0040-4020(99)00057-5

Reference yield: 4.0%

2-methyl-1-buten-4-ol (763-32-6) + 2-methyl-3-buten-2-ol (115-18-4) → geraniol hydrate (27415-10-7) + 1-(3,3-dimethyl-2-propen-1-yl) oxy-3-methyl-3-butene (59637-41-1) + 1-(1,1-dimethyl-2-propen-1-yl) oxy-3-methyl-3-butene

Guidance literature:

With trifluoroacetic acid; In dichloromethane; at 0 ℃; for 0.333333h;

Reference yield:

1-(3,3-dimethyl-2-propen-1-yl) oxy-3-methyl-3-butene (59637-41-1) → 2-methyl-1-buten-4-ol (763-32-6) + 3,7-dimethyl 3,6-octadien-1-ol (7779-06-8) + γ-geraniol (13066-51-8)

Guidance literature:

With (2,6-di-tert-butyl-4-methylphenoxy)methylaluminum trifluoromethanesulfonate; In dichloromethane; at 25 ℃; for 2h; Yield given. Yields of byproduct given;

DOI:10.1016/S0040-4039(00)87225-1

upstream raw materials:

2-methyl-1-buten-4-ol

2-methyl-3-buten-2-ol

3-methyl-2-buten-1-ol

Downstream raw materials:

2-methyl-1-buten-4-ol

3,7-dimethyl 3,6-octadien-1-ol

γ-geraniol